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Title 

Human papillomavirus type 16 E6-specific antitumor immunity is induced by oral administration of HPV16 E6-expressing Lactobacillus casei in C57BL/6 mice

Authors 

Tae Young LeeY H KimK S LeeJeong Ki KimI H LeeJ M YangM H SungJ S ParkHaryoung Poo

Publisher 

Springer Verlag (Germany)

Issue Date 

2010

Citation 

Cancer Immunology, Immunotherapy, vol. 59, no. 11, pp. 1727-1737

Keywords 

Antitumor effectCell-mediated immunityHPV16 E6Lactobacillus caseiPgsA

Abstract 

Given that local cell-mediated immunity (CMI) against the human papillomavirus type 16 E6 (HPV16 E6) protein is important for eradication of HPV16 E6-expressing cancer cells in the cervical mucosa, the HPV16 E6 protein may be a target for the mucosal immunotherapy of cervical cancer. Here, we expressed the HPV16 E6 antigen on Lactobacillus casei (L. casei) and investigated E6-specific CMI following oral administration of the L. casei-PgsA-E6 to mice. Surface expression of HPV16 E6 antigens was confirmed and mice were orally inoculated with the L. casei-PgsA or the L. casei-PgsA-E6. Compared to the L. casei-PgsA-treated mice, significantly higher levels of serum IgG and mucosal IgA were observed in L. casei-PgsA-E6-immunized mice; these differences were significantly enhanced after boost. Consistent with this, systemic and local CMI were significantly increased after the boost, as shown by increased counts of IFN-γ-secreting cells in splenocytes, mesenteric lymph nodes (MLN), and vaginal samples. Furthermore, in the TC-1 tumor model, animals receiving the orally administered L. casei-PgsA-E6 showed reduced tumor size and increased survival rate versus mice receiving control (L. casei-PgsA) immunization. We also found that L. casei-PgsA-E6-induced antitumor effect was decreased by in vivo depletion of CD4+ or CD8+ T cells. Collectively, these results indicate that the oral administration of lactobacilli bearing the surface-displayed E6 protein induces T cell-mediated cellular immunity and antitumor effects in mice.

Citation 

Cancer Immunology, Immunotherapy , 59(11): 1727-1737

ISSN 

0340-7004

Link 

http://dx.doi.org/10.1007/s00262-010-0903-4

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2019-05-02


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